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Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
April 16, 2015
Psychological and practical difficulties among parents and healthy siblings of children with Duchenne vs. Becker muscular dystrophy: an Italian comparative study
Lorenza Magliano, Maria Grazia D'Angelo, Giuseppe Vita, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
February 27, 2026
Respiratory function in Becker muscular dystrophy: a comprehensive longitudinal study
Pietro Riguzzi, Emma Grover, Marianela Schiava, et al.
Neuromuscular Disorders : NMD
|
June 9, 2018
Targeted gene panel screening is an effective tool to identify undiagnosed late onset Pompe disease
Marco Savarese, Annalaura Torella, Olimpia Musumeci, et al.
Brain : a Journal of Neurology
|
September 13, 2021
Clinical and genetic spectrum of a large cohort of patients with δ-sarcoglycan muscular dystrophy
Jorge Alonso-Pérez, Lidia González-Quereda, Claudio Bruno, et al.
Journal of Neurology
|
June 7, 2025
Characterisation of a large, single-centre cohort of patients with Becker muscular dystrophy to inform standardised care guidelines
Pietro Riguzzi, Holly Borland, Meredith K James, et al.
Neuromuscular Disorders : NMD
|
November 9, 2023
Respiratory function in a large cohort of treatment-naïve adult spinal muscular atrophy patients: a cross-sectional study
Alex Vicino, Luca Bello, Silvia Bonanno, et al.
Journal of Neuromuscular Diseases
|
September 18, 2025
Upper limb progression in Duchenne muscular dystrophy: Insights from a 36-month longitudinal study using the PUL 20
Giorgia Coratti, Marika Pane, Sophia Paolucci, et al.
Journal of Neurology
|
May 5, 2022
Genetic modifiers of upper limb function in Duchenne muscular dystrophy
Daniele Sabbatini, Aurora Fusto, Sara Vianello, et al.
Acta Neuropathologica Communications
|
April 16, 2022
Expanding the clinical-pathological and genetic spectrum of RYR1-related congenital myopathies with cores and minicores: an Italian population study
Aurora Fusto, Denise Cassandrini, Chiara Fiorillo, et al.
Neuromuscular Disorders : NMD
|
July 17, 2010
North Star Ambulatory Assessment, 6-minute walk test and timed items in ambulant boys with Duchenne muscular dystrophy
Elena Mazzone, Diego Martinelli, Angela Berardinelli, et al.
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of 15
Search research articles
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Showing results (101-110 of 144) with videos related to
Sort By:
Page
of 15
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
April 16, 2015
Psychological and practical difficulties among parents and healthy siblings of children with Duchenne vs. Becker muscular dystrophy: an Italian comparative study
Lorenza Magliano, Maria Grazia D'Angelo, Giuseppe Vita, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
February 27, 2026
Respiratory function in Becker muscular dystrophy: a comprehensive longitudinal study
Pietro Riguzzi, Emma Grover, Marianela Schiava, et al.
Neuromuscular Disorders : NMD
|
June 9, 2018
Targeted gene panel screening is an effective tool to identify undiagnosed late onset Pompe disease
Marco Savarese, Annalaura Torella, Olimpia Musumeci, et al.
Brain : a Journal of Neurology
|
September 13, 2021
Clinical and genetic spectrum of a large cohort of patients with δ-sarcoglycan muscular dystrophy
Jorge Alonso-Pérez, Lidia González-Quereda, Claudio Bruno, et al.
Journal of Neurology
|
June 7, 2025
Characterisation of a large, single-centre cohort of patients with Becker muscular dystrophy to inform standardised care guidelines
Pietro Riguzzi, Holly Borland, Meredith K James, et al.
Neuromuscular Disorders : NMD
|
November 9, 2023
Respiratory function in a large cohort of treatment-naïve adult spinal muscular atrophy patients: a cross-sectional study
Alex Vicino, Luca Bello, Silvia Bonanno, et al.
Journal of Neuromuscular Diseases
|
September 18, 2025
Upper limb progression in Duchenne muscular dystrophy: Insights from a 36-month longitudinal study using the PUL 20
Giorgia Coratti, Marika Pane, Sophia Paolucci, et al.
Journal of Neurology
|
May 5, 2022
Genetic modifiers of upper limb function in Duchenne muscular dystrophy
Daniele Sabbatini, Aurora Fusto, Sara Vianello, et al.
Acta Neuropathologica Communications
|
April 16, 2022
Expanding the clinical-pathological and genetic spectrum of RYR1-related congenital myopathies with cores and minicores: an Italian population study
Aurora Fusto, Denise Cassandrini, Chiara Fiorillo, et al.
Neuromuscular Disorders : NMD
|
July 17, 2010
North Star Ambulatory Assessment, 6-minute walk test and timed items in ambulant boys with Duchenne muscular dystrophy
Elena Mazzone, Diego Martinelli, Angela Berardinelli, et al.
Page
of 15